posted
Is it my imagination? I always look at the messages to see date that people started lyme net and where they are from. All the doctors who believe this does not exist in their state or does not exist, need only to read this website. For those of you prior to '03 & '04, thanks for helping me with the craze and not feeling alone. My body/mind has a place to go where the 'old ' me is not invited. Unless I speek with someone on LSD, they are lost. Since I left Berkeley Ca. can not find anyone to talk to, Ha! Be well, T. Posts: 61 | From cosmo | Registered: Nov 2004
| IP: Logged |
Beverly
Frequent Contributor (5K+ posts)
Member # 1271
posted
Hi,
I know what you mean...I don't know why so many doctors don't want to belive that there are soo many of us lymies. It makes me nuts too.
caat
Frequent Contributor (1K+ posts)
Member # 2321
posted
yeah, the doctor situation is like being stuck in a Kafka story.
Ya know though, you don't even need an altered state of mind to have the problem you have with not finding many people to talk to after moving out of the Bay Area... Has happened to a lot of us after the great migration...
Posts: 1436 | From Humboldt county ca usa | Registered: Mar 2002
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/